Canonical Allele Identifier: CA478505013

Gene: TNFRSF1A

Linked Data

• gnomAD v4: 12-6333789-G-T
• MyVariant Identifiers: chr12:g.6442955G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6333789G>T , CM000674.2:g.6333789G>T	GRCh38
NC_000012.11:g.6442955G>T , CM000674.1:g.6442955G>T	GRCh37
NC_000012.10:g.6313216G>T	NCBI36
NG_007506.1:g.13307C>A , LRG_193:g.13307C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366159.9:n.304C>A
ENST00000437813.8:c.270C>A	ENSP00000513672.1:p.Thr90=
ENST00000440083.7:c.270C>A	ENSP00000413224.3:p.Thr90=
ENST00000535958.2:c.*97C>A	ENSP00000513673.1:n.*97C>A
ENST00000698339.1:c.270C>A	ENSP00000513670.1:p.Thr90=
ENST00000698340.1:c.270C>A	ENSP00000513671.1:p.Thr90=
ENST00000162749.7:c.270C>A MANE Select	ENSP00000162749.2:p.Thr90=
ENST00000162749.6:c.270C>A	ENSP00000162749.2:p.Thr90=
ENST00000366159.8:c.270C>A	ENSP00000380389.3:p.Thr90=
ENST00000437813.7:n.231C>A
ENST00000440083.6:c.270C>A	ENSP00000413224.2:p.Thr90=
ENST00000534885.5:c.116C>A	ENSP00000441803.1:p.Pro39Gln
ENST00000535958.1:n.516C>A
ENST00000536194.1:c.243C>A	ENSP00000442919.1:p.Thr81=
ENST00000539372.5:c.270C>A	ENSP00000442059.1:p.Thr90=
ENST00000540022.5:c.194-273C>A	ENSP00000438343.1:n.194-273C>A
ENST00000543048.5:c.214+56C>A	ENSP00000439981.1:n.214+56C>A
ENST00000543995.5:c.193+302C>A	ENSP00000442405.1:n.193+302C>A
NM_001065.3:c.270C>A , LRG_193t1:c.270C>A	NP_001056.1:p.Thr90=
NM_001346091.1:c.-55C>A	NP_001333020.1:n.-55C>A
NM_001346092.1:c.-308C>A	NP_001333021.1:n.-308C>A
NR_144351.1:n.573C>A
NM_001065.4:c.270C>A MANE Select	NP_001056.1:p.Thr90=
NM_001346091.2:c.-55C>A	NP_001333020.1:n.-55C>A
NM_001346092.2:c.-308C>A	NP_001333021.1:n.-308C>A
NR_144351.2:n.532C>A